Department of Health Science, Shiga University of Medical Science, Otsu, Japan.
Atherosclerosis. 2011 Mar;215(1):209-13. doi: 10.1016/j.atherosclerosis.2010.11.033. Epub 2010 Dec 4.
The individual components of metabolic syndrome are defined as levels ranging from moderate to high level as to require medication. We investigated the impact of moderate metabolic risk factor clustering on cardiovascular disease (CVD) mortality.
We followed up 6758 non-lean Japanese in randomly selected areas from all over the country who had no history of CVD for 15 years. The multivariate-adjusted hazards ratio (HR) and 95% confidence interval (CI) for CVD mortality according to the number of moderate metabolic risk factors (BMI≥25 kg/m2, 130/85 mmHg≤systolic/diastolic BP<140/90 mmHg, 140 mg/dl≤casual blood glucose<200 mg/dl, triglycerides≥150 mg/dl and/or HDL cholesterol<40 mg/dl [men], 50 mg/dl [women]) were estimated using the Cox proportional hazards model. The population-attributable risk fraction of moderate metabolic risk factor clustering was also estimated.
During the follow-up, 282 participants died of CVD. CVD mortality tended to increase with the number of moderate metabolic risk factors. However, they were not statistically significant. The multivariate-adjusted HRs were 1.82 (95%CI: 0.89-3.73) for having any moderate metabolic risk factors and 2.87 (95%CI: 1.46-5.64) for having any medication-required metabolic risk factors, compared with participants without any moderate metabolic risk factors. The population-attributable risk fractions were 7.3% and 52.4% for any moderate and medication-required metabolic risk factors, respectively.
We did not find the statistically significant increase of CVD mortality for moderate metabolic risk factor clustering. Its attribution was relatively small in this Japanese population. More efforts would be required to detect and control medication-required risk factors.
代谢综合征的各个组成部分被定义为需要药物治疗的中高水平。我们研究了中度代谢危险因素聚集对心血管疾病(CVD)死亡率的影响。
我们对来自全国各地随机选择的非瘦日本人群进行了 15 年的随访,这些人没有 CVD 病史。使用 Cox 比例风险模型估计了根据中度代谢危险因素数量(BMI≥25kg/m2、130/85mmHg≤收缩压/舒张压<140/90mmHg、140mg/dl≤随机血糖<200mg/dl、甘油三酯≥150mg/dl 和/或 HDL 胆固醇<40mg/dl[男性],50mg/dl[女性])的 CVD 死亡率的多变量调整后的风险比(HR)和 95%置信区间(CI)。还估计了中度代谢危险因素聚集的人群归因风险分数。
在随访期间,282 名参与者死于 CVD。CVD 死亡率随着中度代谢危险因素数量的增加而增加,但无统计学意义。与无中度代谢危险因素的参与者相比,有任何中度代谢危险因素的多变量调整后的 HR 为 1.82(95%CI:0.89-3.73),有任何需要药物治疗的代谢危险因素的 HR 为 2.87(95%CI:1.46-5.64)。中度代谢危险因素和需要药物治疗的代谢危险因素的人群归因风险分数分别为 7.3%和 52.4%。
我们没有发现中度代谢危险因素聚集与 CVD 死亡率增加之间存在统计学意义。在这个日本人群中,其归因相对较小。需要更多的努力来检测和控制需要药物治疗的危险因素。